Removal of Bisphenol A Model Compounds and Related Substances Using Octolig®

Bisphenol A used in the production of polycarbonate plastics and epoxy resins is ubiquitous in the environment. The raw material is released to the environment during the manufacturing process and by leaching from consumer products. Recent studies are suggesting that low-dose amounts of Bisphenol A...

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Main Author: Alessio, Rachael Josephine
Format: Others
Published: Scholar Commons 2012
Subjects:
BPA
Online Access:http://scholarcommons.usf.edu/etd/3946
http://scholarcommons.usf.edu/cgi/viewcontent.cgi?article=5142&context=etd
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spelling ndltd-USF-oai-scholarcommons.usf.edu-etd-51422015-09-30T04:42:01Z Removal of Bisphenol A Model Compounds and Related Substances Using Octolig® Alessio, Rachael Josephine Bisphenol A used in the production of polycarbonate plastics and epoxy resins is ubiquitous in the environment. The raw material is released to the environment during the manufacturing process and by leaching from consumer products. Recent studies are suggesting that low-dose amounts of Bisphenol A may have adverse health effects on humans. The possibility of removing Bisphenol A from natural water sources or from solvents used to extract the material from consumer products before they enter the market has been studied. The use of model compounds and related substances (4-isopropylphenol, 4-(t-butyl) phenol, and nitrophenols) have been used to study their removal from aqueous solutions using column chromatography and Octolig®, a commercially available material with polyethylenediamine moieties covalently bonded to high-surface area silica gel. The experimental results suggest that 2-nitrophenol and 4-nitrophenol can be successfully removed while 3-nitrophenol, 4-isopropylphenol, and 4-(t-butyl) phenol did not yield a high percent removal. A look at the pKa of the compounds provides an interesting explanation of the results. It is suggested that the compounds with a pKa of approximately 8.3 or higher would require the solution to be at a high pH for anion formation. The resulting pH of the solution would simultaneously deprotonate the ethylenediamine moieties of Octolig® rendering it incapable of removing the anions by ionic interaction. 2012-01-01T08:00:00Z text application/pdf http://scholarcommons.usf.edu/etd/3946 http://scholarcommons.usf.edu/cgi/viewcontent.cgi?article=5142&context=etd default Graduate Theses and Dissertations Scholar Commons BPA Chromatography Environment Estrogenic Activity Phenols Polycarbonates American Studies Arts and Humanities Chemistry
collection NDLTD
format Others
sources NDLTD
topic BPA
Chromatography
Environment
Estrogenic Activity
Phenols
Polycarbonates
American Studies
Arts and Humanities
Chemistry
spellingShingle BPA
Chromatography
Environment
Estrogenic Activity
Phenols
Polycarbonates
American Studies
Arts and Humanities
Chemistry
Alessio, Rachael Josephine
Removal of Bisphenol A Model Compounds and Related Substances Using Octolig®
description Bisphenol A used in the production of polycarbonate plastics and epoxy resins is ubiquitous in the environment. The raw material is released to the environment during the manufacturing process and by leaching from consumer products. Recent studies are suggesting that low-dose amounts of Bisphenol A may have adverse health effects on humans. The possibility of removing Bisphenol A from natural water sources or from solvents used to extract the material from consumer products before they enter the market has been studied. The use of model compounds and related substances (4-isopropylphenol, 4-(t-butyl) phenol, and nitrophenols) have been used to study their removal from aqueous solutions using column chromatography and Octolig®, a commercially available material with polyethylenediamine moieties covalently bonded to high-surface area silica gel. The experimental results suggest that 2-nitrophenol and 4-nitrophenol can be successfully removed while 3-nitrophenol, 4-isopropylphenol, and 4-(t-butyl) phenol did not yield a high percent removal. A look at the pKa of the compounds provides an interesting explanation of the results. It is suggested that the compounds with a pKa of approximately 8.3 or higher would require the solution to be at a high pH for anion formation. The resulting pH of the solution would simultaneously deprotonate the ethylenediamine moieties of Octolig® rendering it incapable of removing the anions by ionic interaction.
author Alessio, Rachael Josephine
author_facet Alessio, Rachael Josephine
author_sort Alessio, Rachael Josephine
title Removal of Bisphenol A Model Compounds and Related Substances Using Octolig®
title_short Removal of Bisphenol A Model Compounds and Related Substances Using Octolig®
title_full Removal of Bisphenol A Model Compounds and Related Substances Using Octolig®
title_fullStr Removal of Bisphenol A Model Compounds and Related Substances Using Octolig®
title_full_unstemmed Removal of Bisphenol A Model Compounds and Related Substances Using Octolig®
title_sort removal of bisphenol a model compounds and related substances using octolig®
publisher Scholar Commons
publishDate 2012
url http://scholarcommons.usf.edu/etd/3946
http://scholarcommons.usf.edu/cgi/viewcontent.cgi?article=5142&context=etd
work_keys_str_mv AT alessiorachaeljosephine removalofbisphenolamodelcompoundsandrelatedsubstancesusingoctolig
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